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GENE - TERM ANNOTATION REPORT

4 Annotations Found.

An association has been curated linking Snca and Parkinson's disease 1 in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
    		•  
  • The annotation was made from OMIM Disease Annotation Pipeline
  • The annotation has been inferred from sequence orthology with SNCA (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 2 RGD objects have been annotated to Parkinson's disease 1  (DOID:0060367)
  • 75 papers in RGD have been used to annotate Snca


    • An association has been curated linking Snca and Parkinson's disease 1 in Rattus norvegicus.        

  • The association was inferred from sequence or structural similarity (ISS)
    		•  
  • The annotation was made from RGD automated import pipeline for MGI gene-to-disease annotations
  • The annotation has been inferred from sequence or structural similarity with Snca (Mus musculus) [(IAGP) inferred by association of genotype and phenotype]
  • 2 RGD objects have been annotated to Parkinson's disease 1  (DOID:0060367)
  • 75 papers in RGD have been used to annotate Snca
  • Curation Notes: OMIM:168601


    • An association has been curated linking Snca and Parkinson's disease 1 in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
    		•  
  • The annotation was made from RGD automated import pipeline for CTD gene-to-disease annotations
  • The annotation has been inferred from sequence orthology with SNCA (Homo sapiens) [(EXP) inferred from experiment]
  • 2 RGD objects have been annotated to Parkinson's disease 1  (DOID:0060367)
  • 75 papers in RGD have been used to annotate Snca
  • Curation Notes: CTD Direct Evidence: marker/mechanism


    • An association has been curated linking Snca and Parkinson's disease 1 in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred from sequence orthology with SNCA (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 2 RGD objects have been annotated to Parkinson's disease 1  (DOID:0060367)
  • 75 papers in RGD have been used to annotate Snca
  • Curation Notes: ClinVar Annotator: match by term: Autosomal dominant Parkinson disease 1
  • Original References(s): PMID:10417297 PMID:11261505 PMID:11376188 PMID:12062037 PMID:14593171 PMID:14755720 PMID:15144854 PMID:15451224 PMID:15451225 PMID:16358335 PMID:17251522 PMID:17489854 PMID:17625105 PMID:18195271 PMID:18704525 PMID:18852445 PMID:18852448 PMID:18852449 PMID:19632874 PMID:20340137 PMID:20437567 PMID:21252228 PMID:21559878 PMID:23404372 PMID:23427326 PMID:23457019 PMID:23526723 PMID:24047453 PMID:24158904 PMID:24158909 PMID:24313877 PMID:24315198 PMID:24728187 PMID:24746362 PMID:24936070 PMID:24984882 PMID:25268550 PMID:25393002 PMID:25741868 PMID:25892596 PMID:26306801 PMID:26341711 PMID:26799529 PMID:26858591 PMID:27066564 PMID:27393118 PMID:28492532 PMID:29398121 PMID:30528390 PMID:31267130 PMID:33617693 PMID:9197268 PMID:9462735 PMID:9499430 PMID:9506559 PMID:9827625


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